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Clinical Trials/SLCTR/2011/002
SLCTR/2011/002
Recruiting
未知

Intra cervical Foley catheter versus oral misoprostol for pre induction cervical ripening of post dated pregnancies. A randomized controlled trial

niversity of Ruhuna0 sites150 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Effects of Foley catheter versus oral misoprostol for pre-induction cervical ripening
Sponsor
niversity of Ruhuna
Enrollment
150
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
niversity of Ruhuna

Eligibility Criteria

Inclusion Criteria

  • Consecutive women with uncomplicated singleton pregnancies having a cephalic presentation at period of gestation of 40 weeks and 6 days

Exclusion Criteria

  • Complicated pregnancies – both maternal or fetal complications. Pregnancies with uncertain dates not confirmed by early scan, even though clinically considered as 41 weeks. Multiple pregnancies. Pregnancies with contraindication for normal vaginal delivery. Pregnancies with previous caesarean section. Women who have had insertion of intra cervical Foley catheter or vaginal PGE2 before 40 \+ 6 days. Contraindication for the use of misoprostol.

Outcomes

Primary Outcomes

Not specified

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